Canonical Allele Identifier: CA1603685899

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609132_177609136delinsGGTCA , CM000667.2:g.177609132_177609136delinsGGTCA	GRCh38
NC_000005.9:g.177036133_177036137delinsGGTCA , CM000667.1:g.177036133_177036137delinsGGTCA	GRCh37
NC_000005.8:g.176968739_176968743delinsGGTCA	NCBI36
NG_015977.1:g.14015_14019delinsGGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+118_828+122delinsGGTCA MANE Select	ENSP00000029410.5:n.828+118_828+122delinsGGTCA
ENST00000029410.9:c.828+118_828+122delinsGGTCA	ENSP00000029410.5:n.828+118_828+122delinsGGTCA
ENST00000505145.1:n.1926+118_1926+122delinsGGTCA
ENST00000505433.5:c.*334+118_*334+122delinsGGTCA	ENSP00000425591.1:n.*334+118_*334+122delinsGGTCA
ENST00000515353.1:n.1650+118_1650+122delinsGGTCA
NM_007255.2:c.828+118_828+122delinsGGTCA	NP_009186.1:n.828+118_828+122delinsGGTCA
XM_005265805.2:c.486+118_486+122delinsGGTCA	XP_005265862.1:n.486+118_486+122delinsGGTCA
XM_006714816.2:c.348+118_348+122delinsGGTCA	XP_006714879.1:n.348+118_348+122delinsGGTCA
XM_011534421.1:c.486+118_486+122delinsGGTCA	XP_011532723.1:n.486+118_486+122delinsGGTCA
XM_006714816.4:c.348+118_348+122delinsGGTCA	XP_006714879.1:n.348+118_348+122delinsGGTCA
XM_017008999.2:c.486+118_486+122delinsGGTCA	XP_016864488.1:n.486+118_486+122delinsGGTCA
NM_007255.3:c.828+118_828+122delinsGGTCA MANE Select	NP_009186.1:n.828+118_828+122delinsGGTCA